The prevalence of factor V Leiden (G1691A) and methylenetetrahydrofolate reductase C677T mutations in sickle cell disease in Western India
HK Kangne, FF Jijina, YM Italia… - Clinical and Applied …, 2015 - journals.sagepub.com
The prevalence of the Factor V Leiden (FVL; G1691A) mutation and the
methylenetetrahydrofolate reductase (MTHFR; C677T) mutation was determined in 180 …
methylenetetrahydrofolate reductase (MTHFR; C677T) mutation was determined in 180 …
[HTML][HTML] Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy
Juvenile myoclonic epilepsy (JME) accounts for 26% of generalized idiopathic epileptic
syndromes. The highest levels of thrombin activity are closely involved in the development of …
syndromes. The highest levels of thrombin activity are closely involved in the development of …
Coagulopathies
FJ Kirkham - Rosenberg's Molecular and Genetic Basis of …, 2015 - Elsevier
Several genes predisposing to thrombosis have been identified and extensively investigated
as contributors to the risk of stroke at all ages and of dementia and other neurodegenerative …
as contributors to the risk of stroke at all ages and of dementia and other neurodegenerative …